The present disclosure relates to the field of medical first-aid supplies, in particular to an artificial respiration apparatus for first aid.
When someone has a cardiac arrest, the success rate of rescue can be improved by timely cardiac compression and artificial respiration. However, during performing of artificial respiration, a rescuer needs to bend over and kneel down, hold the nose of a person to be rescued with one hand, and completely wrap the mouth of the person to be rescued to blow air. There are several problems during the process.
Firstly, when the rescuer kneels down and bends over, the exertion of blowing is not facilitated, and the condition of the person to be rescued is not easy to observe.
Secondly, due to mouth-to-mouth artificial respiration, the rescuer may suffer from the risk of infection. At the same time, the droplets of the rescuer are easy to blow into the mouth of the person to be rescued.
Thirdly, some rescuers psychologically conflict with contact with the mouth of the person to be rescued, so that timely and effective artificial respiration is not developed smoothly.
At present, there are disposable barrier respiration membranes for artificial respiration in the market, which can isolate direct mouth contact between the rescuer and the person to be rescued and reduce the risk of cross infection. However, there are still some problems. For example, the blown force is poor. The sealing performance is low. The mouth of the rescuer needs to be close to the mouth of the person to be rescued. The mouth of the rescuer completely wraps the mouth of the person to be rescued to blow air. The present disclosure provides an artificial respiration apparatus for first aid so as to solve the problems proposed in the background technology.
The purpose of the present disclosure is to provide an artificial respiration apparatus for first aid so as to solve the problems proposed in the background technology.
In order to achieve the above purposes, the present disclosure provides the following technical scheme.
An artificial respiration apparatus for first aid includes an adhesive film, wherein a fixing block is provided on an upper end of the adhesive film, a first adhesive strip is provided on a lower end of the adhesive film, a second adhesive strip is also provided on the lower end of the adhesive film, and a blowing device is inserted in the fixing block; and
the blowing device includes a ventilation pipe, one end of the ventilation pipe passes through the adhesive film and the fixing block in sequence from the lower end of the adhesive film, a first connecting block is provided on the other end of the ventilation pipe, an intraoral ventilation pipe is provided on one end, away from the ventilation pipe, of the first connecting block, a second connecting block is provided on one end, close to the first connecting block, of the intraoral ventilation pipe, the intraoral ventilation pipe is connected with the ventilation pipe through the second connecting block and the first connecting block, a connecting pipe is provided on the upper end of the ventilation pipe and located above the fixing block, an air inlet pipe is provided on one end, away from the ventilation pipe, of the connecting pipe, a filter is provided on one end, away from the connecting pipe, of the air inlet pipe, a blowing port is formed in one end, away from the air inlet pipe, of the filter, a bypass pipe is provided on one side of the ventilation pipe, the upper end of the bypass pipe passes through the adhesive film and the fixing block in sequence, and a protective plug is provided on the upper end of the bypass pipe.
In some embodiments, a plurality of bundling belts are provided on an upper end of the fixing block.
In some embodiments, the second adhesive strip is set as a triangle.
In some embodiments, a blowing cover is provided on one end, away from the filter, of the blowing port.
In some embodiments, a plurality of adhesive tapes are provided on the upper end of the adhesive film, one end of each adhesive tape is fixedly connected with the adhesive film, and the other end of the adhesive tape is adhered with the adhesive film.
In some embodiments, a ventilation port is formed in a surface of the intraoral ventilation pipe, and the ventilation port passes through a shell wall of the intraoral ventilation pipe.
In some embodiments, a double-sided adhesive tape is provided on a lower end of the fixing block, and the fixing block is bonded and connected with the adhesive film through the double-sided adhesive tape.
In some embodiments, an adhesive area is provided on the upper end of the adhesive film and located below the fixing block, and a connecting port is formed inside the adhesive area.
Compared with the prior art, the present disclosure has the following beneficial effects.
Firstly, when the apparatus is used, the intraoral ventilation pipe is inserted into the mouth of a person to be rescued, the intraoral ventilation pipe is bypassed around the tongue of the person to be rescued to prevent the tongue of the person to be rescued from blocking the trachea. Then the adhesive film is applied to the mouth and nose of the person to be rescued. After the adhesive film is adhered to the mouth and nose of the person to be rescued, and through the first adhesive strip and the second adhesive strip, the connecting strength between the adhesive film and the face of the person to be rescued is increased. Finally, air is blown into the blowing port, such that the blown air enters the body of the person to be rescued through the ventilation pipe and the intraoral ventilation pipe, so as to prevent a rescuer from kneeling on the ground or lying prostrate to perform artificial respiration for the person to be rescued, and also prevent the mouth of the rescuer from contacting the mouth of the person to be rescued, thereby making the artificial respiration easier and simpler.
Secondly, after the person to be rescued spontaneously breathes, the adhesive film is torn off from the face of the person to be rescued, then the adhesive film is torn off from the fixing block, the torn adhesive film is discarded, and the blowing device is reserved. By disinfecting the blowing device, the blowing device can be used repeatedly, so that the practicability of the apparatus is improved.
The apparatus has the characteristics of simple structure and convenience in use.
Reference signs: 1, adhesive film; 100, adhesive area; 101, connecting port; 2, fixing block; 200, double-sided adhesive tape; 201, bundling belt; 3, first adhesive strip; 4, second adhesive strip; 5, ventilation pipe; 500, first connecting block; 501, intraoral ventilation pipe; 502, second connecting block; 503, ventilation port; 6, bypass pipe; 7, protective plug; 700, pressure relief hole; 701, barrier block; 702, connector; 703, baffle; 704, spring; 8, connecting pipe; 9, air inlet pipe; 10, filter; 11, blowing port; 110, blowing cover; and 12, adhesive tape.
The following clearly and completely describes the technical scheme in the embodiments of the present disclosure with reference to the attached figures in the embodiments of the present disclosure. Apparently, the described embodiments are merely a part rather than all of the embodiments of the present disclosure. Based on the embodiment in the present disclosure, all other embodiments obtained by the ordinary technical staff in the art under the premise of without contributing creative labor belong to the scope protected by the present disclosure.
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In this embodiment, a plurality of bundling belts 201 are provided on the upper end of the fixing block 2. The bundling belt 201 is of elasticity. The bonding strength of the first adhesive strip 3, the second adhesive strip 4 and the adhesive film 1 with the nose and mouth can be enhanced through the bundling belts 201.
In this embodiment, the second adhesive strip 4 is set as a triangle. The second adhesive strip 4 is set as a triangle to facilitate the second adhesive strip 4 to be attached to the nose of a person to be rescued.
In this embodiment, a plurality of adhesive tapes 12 are provided on the upper end of the adhesive film 1. One end of the adhesive tape 12 is fixedly connected with the adhesive film 1, and the other end of the adhesive tape 12 is adhered with the adhesive film 1. The connecting pipe 8 is bent so that the air inlet pipe 9 is bonded to the surface of the adhesive film 1, and then the air inlet pipe 9 is fixed to the surface of the adhesive film 1 through the adhesive tape 12, thereby reducing the occupied space of the apparatus. The apparatus is easier to carry.
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The working process of the present disclosure is as follows.
When the apparatus is used, the intraoral ventilation pipe 501 is firstly inserted into the mouth of the person to be rescued. The intraoral ventilation pipe 501 is bypassed around the tongue of the person to be rescued to prevent the tongue of the person to be rescued from blocking the trachea. Then, the adhesive film 1 is applied to the mouth and nose of the person to be rescued. After the adhesive film 1 is adhered to the mouth and nose of the person to be rescued, and through the first adhesive strip and the second adhesive strip, the connecting strength between the adhesive film 1 and the face of the person to be rescued is increased. The bundling belts 201 are bypassed around the neck to be fixed, so that the bonding strength between the adhesive film 1 and the face of the person to be rescued is further increased. Finally, air is blown into the blowing port 11. The blown air enters the body of the person to be rescued through the ventilation pipe 5 and the intraoral ventilation pipe 501. The ventilation port 503 in the intraoral ventilation pipe 501 can prevent the tongue from blocking the air inlet of the intraoral ventilation pipe 501. When it is necessary to pump out liquid accumulated in the oral cavity of the person to be rescued, a pipette can be inserted into the oral cavity through the bypass pipe 6, and then the liquid in the oral cavity of the person to be rescued can be sucked out by using the pipette.
After the person to be rescued spontaneously breathes, the adhesive film 1 is torn off from the face of the person to be rescued, then the adhesive film 1 is torn off from the fixing block 2, the torn adhesive film 1 is discarded, and the blowing device is reserved. By disinfecting the blowing device, the blowing device can be used repeatedly.
The above mentioned are only preferred specific embodiments of the present disclosure. However, the scope of protection of the present disclosure is not limited to the embodiments described herein. Any technicians skilled in the technical field are within the technical scope disclosed by the present disclosure; and any replacements or modifications according to the technical schemes of the present disclosure and ideas thereof all shall be included in the scope of protection of the present disclosure.
Number | Date | Country | Kind |
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202110609663.3 | Jun 2021 | CN | national |
Filing Document | Filing Date | Country | Kind |
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PCT/CN2022/096108 | 5/31/2022 | WO |